Canonical Allele Identifier: CA309445944
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs899039504
gnomAD v2: 19-49564073-A-C
gnomAD v3: 19-49060816-A-C
gnomAD v4: 19-49060816-A-C
MyVariant Identifiers: chr19:g.49564073A>C (hg19) chr19:g.49060816A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060816A>C , CM000681.2:g.49060816A>C GRCh38
NC_000019.9:g.49564073A>C , CM000681.1:g.49564073A>C GRCh37
NC_000019.8:g.54255885A>C NCBI36
NG_016289.1:g.8052T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+939T>G ENSP00000470689.1:n.243+939T>G
XM_011527575.1:c.-64T>G XP_011525877.1:n.-64T>G
XR_001753693.1:n.879+348T>G
XR_001753694.1:n.880-7T>G
Search 100 bp 5'
Search 100 bp 3'